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Maxi-probe Irrigation Needle

FDA UDI

Class I (US FDA UDI)

by Tulsa Dental Products Llc

Identity

Trade Name
Maxi-probe Irrigation Needle FDA UDI
Generic Name
Dental syringe needle, single-use FDA UDI
Device Name
Max-i-Probe® 23GA. 40 PK FDA UDI
Model / Reference
MAXP234 FDA UDI
Description
Max-i-Probe® 23GA. 40 PK FDA UDI

Identifiers

Catalog Number
MAXP234 FDA UDI
Primary DI / UDI-DI
D716MAXP2341 FDA UDI
FDA Product Code
EIC FDA UDI
GMDN Term
Dental syringe needle, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental syringe needle, single-use

Maxi-probe Irrigation Needle by Tulsa Dental Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental syringe needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 624bce38-70da-4e85-9fb7-b7478c86e314 34 fields · synced May 31, 2026